Variant report

Variant rs10497318
Chromosome Location chr2:168037315-168037316
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168032600-168037600 Weak transcription Gastric stomach
2 chr2:168034200-168037400 Weak transcription Osteobl bone
3 chr2:168034400-168037400 Weak transcription HSMM muscle
4 chr2:168034400-168038600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr2:168034600-168037400 Weak transcription NHDF-Ad bronchial
6 chr2:168035000-168037400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr2:168035400-168037400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr2:168036400-168039000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr2:168037000-168037400 Enhancers Muscle Satellite Cultured Cells --
10 chr2:168037200-168038000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:168037200-168038800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr2:168037200-168039000 Enhancers NHEK skin
13 chr2:168037200-168039200 Enhancers HMEC breast
14 chr2:168037200-168039200 Enhancers NHLF lung

Quick Search:


  
Input of quick search could be:

what's new

Quick links